HIV InfectionNCT02102724
Fish Oil for HIV-Related Inflamm-aging and Immune Senescence
A study testing Fish oil that contains omega-3 fatty acids in people with HIV Infection, run by Rush University Medical Center at 1 site in United States.
Trial summary
HIV infection is associated with premature aging of the immune system. It is believe that the persistent inflammation that accompanies HIV infection is a major contributor to premature immune aging. Fish oil has well-documented anti-inflammatory properties. Read more about this study
- Who is it for?
- Ages 40 to 70 years
- Conditions the study is for
- HIV Infection
- What is being tested?
- Fish oil that contains omega-3 fatty acids
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 37 participants
- Where
- 1 siteUnited States
- Study dates
- Apr 2014to Dec 2015
- Phase
- Interventional
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- documented HIV infection
- between 40 and 70 years of age
- clinically stable HIV disease as evidenced by a CD4+ T lymphocyte count of > 250 cells/mm3
- platelet count between 150,000 and 400,000 cells/mm3 to reduce bleeding risks associated with omega 3-fatty acids
- treatment with a stable HAART regimen for at least six months prior to study entry
- plasma HIV RNA < 75 copies/ml for at least 12 months
- elevated plasma concentration of hsCRP (> 2.0 mg/L).
Who cannot join
- use within the past month of drugs (e.g., statins, steroids, hormones) and supplements (e.g., omega-3 fatty acids, glucosamine/chondroitin) that have anti-inflammatory effects (excluding non-regular use of aspirin or NSAIDS), or medications or supplements that affect bleeding (e.g., heparin, warfarin, clopidogrel, garlic, ginseng)
- allergy to fish or shellfish
- chronic inflammatory condition (e.g., asthma, rheumatoid arthritis), opportunistic infection or cancer, renal impairment (serum creatinine > 2.0 mg/dL), thrombocytopenia (platelet count < 150,000/mm3), bleeding episodes (e.g., gum bleeding, nosebleeds), or a metabolic condition (e.g., diabetes mellitus, thyroid disease)
- body mass index of > 35, since obesity is associated with inflammation
- impaired liver function as evidenced by liver enzyme elevations > three times the upper limit of normal (AST or ALT > 150 IU/L)
- history of prostate cancer
- LDL cholesterol level > 120 mg/dL
- lifestyle exclusion factors include use of illicit drugs and consumption of > 3 alcoholic drinks/day
Trial locations and contacts
1 site in 1 country.
United States1 site
Rush University Medical Center
Chicago, Illinois, 60612
About this study
HIV infection is associated with premature aging of the immune system. It is believe that the persistent inflammation that accompanies HIV infection is a major contributor to premature immune aging. Fish oil has well-documented anti-inflammatory properties. In this randomized, clinical trial, we're testing whether a 12-week course of fish oil supplementation will reverse premature aging in HIV-infected older adults.
Read the detailed description
Due to treatment advances, the number of persons > 50 years old who are living with HIV/AIDS in the United States (US) has steadily increased. African Americans (AA) represent a disproportionate number of HIV/AIDS cases in this age group, with infection rates 12 times higher than among whites (51.7 per 100,000 compared to 4.2 per 100,000). Limited data suggest that older HIV+ AA are characterized by health status disparities. One cohort study of older, largely minority HIV+ persons (N=121, AA=83%;mean age=54), found that 34% had metabolic syndrome and 50% had a Framingham Cardiac Risk score > 10%. HIV+ older adults of all races show a premature onset of other age-associated co-morbidities, such as osteoporosis, non-AIDS malignancies, and cardiovascular disease (CVD). These co-morbidities have been linked to persistent inflammation and persistently elevated serum levels of proinflammatory cytokines that mimic an aging phenotype known as "inflamm-aging." In both middle-aged HIV+ persons and older HIV seronegative adults, inflamm-aging is associated with more limited T cell repertoires and increased risk for morbidities and mortality. In HIV infection, inflamm-aging is postulated to be maintained (a) by the constant antigen burden imposed by HIV and other chronic viral co-pathogens, such as cytomegalovirus (CMV), and (b) by HIV-induced disruption of intestinal epithelial integrity with subsequent translocation of gut microflora into the systemic circulation. Our hypothesis is that inflamm-aging is responsible for the premature immune senescence associated with HIV infection in aging individuals. Immune senescence, characterized by diminished replicative capacity, has been observed in middle-aged persons treated with highly active antiretroviral therapy (HAART) who achieve immune reconstitution and undetectable viral loads. Senescent cells are characterized by the absence of the surface marker CD28, and in advanced senescence express CD57 (CD28-/CD57+ phenotype). Because premature senescence leads to loss of anti-HIV cell-mediated immune responses and accelerated HIV disease progression,there is an urgent need to test new treatment strategies to reduce inflamm-aging and subsequent immune senescence.
Fish oil may be an effective treatment option for reducing HIV-related inflamm-aging. Cold water fish are rich in the omega-3 highly unsaturated fatty acids (HUFA) eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which have anti-inflammatory effects. When consumed as fish or fish oil supplements, EPA and DHA replace arachidonic acid in cell membranes and inhibit the synthesis of proinflammatory arachidonic acid metabolites, such as prostaglandins and leukotrienes. Moreover, animal and in vitro studies have shown that EPA and DHA stimulate regeneration of intestinal mucosa damaged by methotrexate,16 IL-4, and experimental ulcerative colitis. Yet, to date, no studies have been conducted on the effects of fish oil for reducing HIV-related inflamm-aging and reversing immune senescence.
The purpose of this study is to explore the safety and estimate the effect size of fish oil to modulate parameters of inflamm-aging and immune senescence in HIV+ older adults. Participants will receive either 1.6 grams of omega-3 fatty acids (800 mg of EPA, 600 mg DHA, 200 mg other omega-3 fatty acids) or placebo for 12 weeks. We expect to find a reduction in inflammatory markers and the percentage of CD8+ and CD4+ T lymphocytes that exhibit a senescent phenotype in the fish oil condition, but not in the control condition, at 12 weeks. We expect to find no difference between the conditions on the safety parameters at 4 and 12 weeks.
The specific aims are:
Aim 1. To assess the safety of the fish oil condition by comparing it to the control condition at 4 and 12 weeks, controlling for covariates (demographics, lifestyle, medications including HAART, fish oil supplement adherence, intercurrent illnesses), on
- HIV disease parameters (CD4+ T cell counts and HIV RNA levels)
- Drug toxicity (liver function tests and serum creatinine)
- Adverse events (e.g., diarrhea, vomiting)
Aim 2. To estimate the effect size of the fish oil condition at 12 weeks, controlling for covariates, by comparing the following cell surface molecules and intracellular and soluble inflammatory markers before and after fish oil
- Markers of immune senescence on CD8+ T lymphocytes: percentage of CD8+/CD28- T lymphocytes, a phenotype of immune senescence (primary outcome); percentage of CD8+/CD28-/CD57- T lymphocytes (an intermediate senescent phenotype); percentage of CD8+/CD28-/CD57+ T lymphocytes (a terminally differentiated senescent phenotype)
- Markers of immune senescence on CD4+ T lymphocytes: percentage of CD4+/CD28- T lymphocytes; percentage of CD4+/CD28-/CD57- T lymphocytes; percentage of CD4+/CD28-/CD57+ T lymphocytes
- Markers of inflammation: plasma hsCRP and intracellular concentrations of TNF-alpha, IL-6, and gamma IFN
Aim 3: To estimate the effect size of the fish oil condition at 12 weeks on gut permeability, controlling for covariates, by comparing the following indirect markers of gut permeability before and after fish oil
- Endotoxin
- Soluble mouse CD14
- Endotoxin binding antibody
- Lipopolysaccharide binding protein
- Conditions
- HIV Infection
- Being tested
- Fish oil that contains omega-3 fatty acids, Placebo
- Keywords
- African Americans, Older Adults
- Medical subject headings
- HIV Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Fish oil that contains omega-3 fatty acidsDietary supplement
Also called Carlson Brand fish oil
Fish oil gelcaps that contain 800 mg of EPA, 600 mg of DHA, 200 mg other omega-3 fatty acids
PlaceboDietary supplement
Gelcaps that contain 1 gram of oleic sunflower oil
| Study group | Role | What they receive |
|---|---|---|
| Fish Oil | Experimental | Participants will receive fish oil gelcaps that contain 1.6 grams of omega-3 fatty acids (800 mg of EPA, 600 mg DHA, 200 mg other omega-3 fatty acids) for 12 weeks. Receives: Dietary Supplement: Fish oil that contains omega-3 fatty acids |
| Placebo | Placebo comparator | Participants will receive 1 gram of oleic sunflower oil for 12 weeks. Receives: Dietary Supplement: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Markers of Immune Senescence Between Baseline Values and Values After 12 Weeks of Supplementation
Markers of immune senescence will include change in the expression of the senescence markers CD28 and CD57 on the surface of peripheral CD4+ and CD8+ T lymphocytes. We will measure the percentage of CD4+ and CD8+ T lymphocytes that are CD28-/CD57- or CD28-/CD57+. We will subtract the percentage obtained at Week 12 from the baseline percentage to calculate the change scores.
Measured: End of 12-Week Supplementation Period
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Apr 2014 (estimated)
- Study startApr 2014
- Primary completionDec 2015
- Study completionDec 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for HIV InfectionStudies of the same condition, open and under way.
- More trials run by Rush University Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Participants were randomized to one of two arms: Intervention arm = fish oil Control arm = placebo.
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 37 participants (actual)
Sponsor and investigators
- Lead sponsor
- Rush University Medical Center
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Barbara A. Swanson, PhD, RN, Principal investigator, Rush University College of Nursing
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02102724
- Sponsor's protocol ID
- 5P20MD006886
- Status last verified
- Mar 2019
- First submitted
- 31 Mar 2014
- Last updated
- 26 Mar 2019
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Mar 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Fish Oil for HIV-Related Inflamm-aging and Immune Senescence
- ClinicalTrials.gov ID
- NCT02102724
- Acronym / sponsor ID
- 5P20MD006886
- Conditions
- HIV Infection
- Keywords
- African Americans, Older Adults
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 37 participants (actual)
- Lead sponsor
- Rush University Medical CenterUniversity, hospital or other
- Study start
- Apr 2014
- Primary completion
- Dec 2015 (actual)
- Study completion
- Dec 2015 (actual)
- First posted
- 3 Apr 2014 (estimated)
- Results
- Posted 26 Mar 2019
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
HIV infection is associated with premature aging of the immune system. It is believe that the persistent inflammation that accompanies HIV infection is a major contributor to premature immune aging. Fish oil has well-documented anti-inflammatory properties. In this randomized, clinical trial, we're testing whether a 12-week course of fish oil supplementation will reverse premature aging in HIV-infected older adults.
Detailed description
Due to treatment advances, the number of persons > 50 years old who are living with HIV/AIDS in the United States (US) has steadily increased. African Americans (AA) represent a disproportionate number of HIV/AIDS cases in this age group, with infection rates 12 times higher than among whites (51.7 per 100,000 compared to 4.2 per 100,000). Limited data suggest that older HIV+ AA are characterized by health status disparities. One cohort study of older, largely minority HIV+ persons (N=121, AA=83%;mean age=54), found that 34% had metabolic syndrome and 50% had a Framingham Cardiac Risk score > 10%. HIV+ older adults of all races show a premature onset of other age-associated co-morbidities, such as osteoporosis, non-AIDS malignancies, and cardiovascular disease (CVD). These co-morbidities have been linked to persistent inflammation and persistently elevated serum levels of proinflammatory cytokines that mimic an aging phenotype known as "inflamm-aging." In both middle-aged HIV+ persons and older HIV seronegative adults, inflamm-aging is associated with more limited T cell repertoires and increased risk for morbidities and mortality. In HIV infection, inflamm-aging is postulated to be maintained (a) by the constant antigen burden imposed by HIV and other chronic viral co-pathogens, such as cytomegalovirus (CMV), and (b) by HIV-induced disruption of intestinal epithelial integrity with subsequent translocation of gut microflora into the systemic circulation. Our hypothesis is that inflamm-aging is responsible for the premature immune senescence associated with HIV infection in aging individuals. Immune senescence, characterized by diminished replicative capacity, has been observed in middle-aged persons treated with highly active antiretroviral therapy (HAART) who achieve immune reconstitution and undetectable viral loads. Senescent cells are characterized by the absence of the surface marker CD28, and in advanced senescence express CD57 (CD28-/CD57+ phenotype). Because premature senescence leads to loss of anti-HIV cell-mediated immune responses and accelerated HIV disease progression,there is an urgent need to test new treatment strategies to reduce inflamm-aging and subsequent immune senescence.
Fish oil may be an effective treatment option for reducing HIV-related inflamm-aging. Cold water fish are rich in the omega-3 highly unsaturated fatty acids (HUFA) eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which have anti-inflammatory effects. When consumed as fish or fish oil supplements, EPA and DHA replace arachidonic acid in cell membranes and inhibit the synthesis of proinflammatory arachidonic acid metabolites, such as prostaglandins and leukotrienes. Moreover, animal and in vitro studies have shown that EPA and DHA stimulate regeneration of intestinal mucosa damaged by methotrexate,16 IL-4, and experimental ulcerative colitis. Yet, to date, no studies have been conducted on the effects of fish oil for reducing HIV-related inflamm-aging and reversing immune senescence.
The purpose of this study is to explore the safety and estimate the effect size of fish oil to modulate parameters of inflamm-aging and immune senescence in HIV+ older adults. Participants will receive either 1.6 grams of omega-3 fatty acids (800 mg of EPA, 600 mg DHA, 200 mg other omega-3 fatty acids) or placebo for 12 weeks. We expect to find a reduction in inflammatory markers and the percentage of CD8+ and CD4+ T lymphocytes that exhibit a senescent phenotype in the fish oil condition, but not in the control condition, at 12 weeks. We expect to find no difference between the conditions on the safety parameters at 4 and 12 weeks.
The specific aims are:
Aim 1. To assess the safety of the fish oil condition by comparing it to the control condition at 4 and 12 weeks, controlling for covariates (demographics, lifestyle, medications including HAART, fish oil supplement adherence, intercurrent illnesses), on
- HIV disease parameters (CD4+ T cell counts and HIV RNA levels)
- Drug toxicity (liver function tests and serum creatinine)
- Adverse events (e.g., diarrhea, vomiting)
Aim 2. To estimate the effect size of the fish oil condition at 12 weeks, controlling for covariates, by comparing the following cell surface molecules and intracellular and soluble inflammatory markers before and after fish oil
- Markers of immune senescence on CD8+ T lymphocytes: percentage of CD8+/CD28- T lymphocytes, a phenotype of immune senescence (primary outcome); percentage of CD8+/CD28-/CD57- T lymphocytes (an intermediate senescent phenotype); percentage of CD8+/CD28-/CD57+ T lymphocytes (a terminally differentiated senescent phenotype)
- Markers of immune senescence on CD4+ T lymphocytes: percentage of CD4+/CD28- T lymphocytes; percentage of CD4+/CD28-/CD57- T lymphocytes; percentage of CD4+/CD28-/CD57+ T lymphocytes
- Markers of inflammation: plasma hsCRP and intracellular concentrations of TNF-alpha, IL-6, and gamma IFN
Aim 3: To estimate the effect size of the fish oil condition at 12 weeks on gut permeability, controlling for covariates, by comparing the following indirect markers of gut permeability before and after fish oil
- Endotoxin
- Soluble mouse CD14
- Endotoxin binding antibody
- Lipopolysaccharide binding protein
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 2
- Model description
- Participants were randomized to one of two arms: Intervention arm = fish oil Control arm = placebo.
| Arm | Type | Receives |
|---|---|---|
| Fish Oil | Experimental | Dietary Supplement: Fish oil that contains omega-3 fatty acidsParticipants will receive fish oil gelcaps that contain 1.6 grams of omega-3 fatty acids (800 mg of EPA, 600 mg DHA, 200 mg other omega-3 fatty acids) for 12 weeks. |
| Placebo | Placebo comparator | Dietary Supplement: PlaceboParticipants will receive 1 gram of oleic sunflower oil for 12 weeks. |
Who may qualify
- Ages
- 40 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- documented HIV infection
- between 40 and 70 years of age
- clinically stable HIV disease as evidenced by a CD4+ T lymphocyte count of > 250 cells/mm3
- platelet count between 150,000 and 400,000 cells/mm3 to reduce bleeding risks associated with omega 3-fatty acids
- treatment with a stable HAART regimen for at least six months prior to study entry
Key exclusion criteria (8 listed)
- use within the past month of drugs (e.g., statins, steroids, hormones) and supplements (e.g., omega-3 fatty acids, glucosamine/chondroitin) that have anti-inflammatory effects (excluding non-regular use of aspirin or NSAIDS), or medications or supplements that affect bleeding (e.g., heparin, warfarin, clopidogrel, garlic, ginseng)
- allergy to fish or shellfish
- chronic inflammatory condition (e.g., asthma, rheumatoid arthritis), opportunistic infection or cancer, renal impairment (serum creatinine > 2.0 mg/dL), thrombocytopenia (platelet count < 150,000/mm3), bleeding episodes (e.g., gum bleeding, nosebleeds), or a metabolic condition (e.g., diabetes mellitus, thyroid disease)
- body mass index of > 35, since obesity is associated with inflammation
- impaired liver function as evidenced by liver enzyme elevations > three times the upper limit of normal (AST or ALT > 150 IU/L)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Fish oil that contains omega-3 fatty acidsAlso: Carlson Brand fish oilFish oil gelcaps that contain 800 mg of EPA, 600 mg of DHA, 200 mg other omega-3 fatty acids | Dietary supplement | Fish Oil |
| PlaceboGelcaps that contain 1 gram of oleic sunflower oil | Dietary supplement | Placebo |
Primary outcome
Change in Markers of Immune Senescence Between Baseline Values and Values After 12 Weeks of Supplementation
Time frame: End of 12-Week Supplementation Period
Markers of immune senescence will include change in the expression of the senescence markers CD28 and CD57 on the surface of peripheral CD4+ and CD8+ T lymphocytes. We will measure the percentage of CD4+ and CD8+ T lymphocytes that are CD28-/CD57- or CD28-/CD57+. We will subtract the percentage obtained at Week 12 from the baseline percentage to calculate the change scores.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Mar 2019.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Barbara A. Swanson, PhD, RN principal investigator
Rush University College of Nursing
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Fish oil that contains omega-3 fatty acids in people with HIV Infection, run by Rush University Medical Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 Mar 2019. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Yes. Results are posted in the registry (first posted 26 Mar 2019). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in Markers of Immune Senescence Between Baseline Values and Values After 12 Weeks of Supplementation (time frame: End of 12-Week Supplementation Period). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Mar 2019.